Veterans helping veterans: new study aims to stop suicide
NCT ID NCT07286383
First seen Jun 27, 2026 · Last updated Sep 09, 2026 · Updated 5 times
Summary
This study tests a new program called PREVAIL-VA, where trained peer specialists—veterans who have their own mental health challenges—provide one-on-one support to fellow veterans at risk for suicide. Over 3 months, 306 veterans will receive either this peer support or usual care. The goal is to see if talking with someone who truly understands can reduce suicide risk and improve recovery.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 306 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2026
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: There are two Inclusion criteria: * Moderate to high suicide risk according to one of the following occurring in the prior 3 months: * a completed Comprehensive Suicide Risk Evaluation (CSRE) indicating intermediate or high acute or chronic risk * a high-risk suicide PRF * a suicide attempt indicated on a Suicide Behavior or Overdose Report (SBOR) * a suicide safety plan completed in the past 6 months AND * Current suicidal ideation according to the 9th item of the Patient health questionnaire (PHQ-9) \> 0 at enrollment * While a positive 9th item usually precedes the CSRE, because the CSRE could have been administered in the 3 months prior to enrollment, the purpose of requiring a positive 9th item is to ensure more recent suicidal ideation. * It may be more difficult to show an intervention effect if the investigators enroll participants with no suicidal ideation at baseline. Exclusion Criteria: * Inability to provide informed consent for any reason, including due to acute psychosis or mania, dementia, or active guardianship or durable power of attorney * These criteria will be determined according to medical record review and, if clarification needed, consultation with a treating provider. * The investigators will also screen for decision-making capacity using the Blessed Orientation, Memory, Concentration (BOMC) Test and a brief quiz about the study. * This quiz will involve an iterative process of querying the participants' understanding of consent information with a 10-item true/false test and providing feedback until an acceptable level of understanding is achieved (must get 100% correct after 3 tries to enroll). * Current or planned receipt of residential or intensive outpatient treatment * Plan to transfer or terminate care in the next 3 months * Homicidal ideation in the past 6 months or violent behavior in the past 12 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD
RECRUITINGBaltimore, Maryland, 21201, United States
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VA Ann Arbor Healthcare System, Ann Arbor, MI
ACTIVE_NOT_RECRUITINGAnn Arbor, Michigan, 48105-2303, United States
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VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
RECRUITINGPittsburgh, Pennsylvania, 15240, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a talk therapy that boosts Self-Understanding prevent suicide?
- Can data sharing prevent suicide among Jail-Cycling individuals?
- Writing away the pain: Text-Based therapy tested for suicidal youth
- App + therapy shows promise in cutting suicide risk for eating disorder patients
- Could a One-Hour talk save lives? new trial tests crisis planning for soldiers with brain injury